”To develop bottromycins further, the producing bacteria need to be persuaded to make new versions of bottromycin that have improved properties,“ says Jun.-Prof. Jesko Köhnke, who heads the junior research group ”Structural Biology of Biosynthetic Enzymes“ at HIPS. For this, however, the scientists must first understand how the complicated chemical reactions during the formation of bottromycin are performed within the bacterial cell in detail. Together with Prof. Iris Antes' research group at the Technical University of Munich, Köhnke's team has now presented a detailed study on the enzyme PurAH, which plays an important role in the production of bottromycin. In addition to the reaction performed by this enzyme, the scientists have also determined its three-dimensional structure at the atomic level. They found PurAH to collaborate with another bottromycin enzyme, which places PurAH as the gatekeeper of bottromycin biosynthesis. These findings will be important in future efforts to produce improved bottromycins. The scientists published their results in the renowned Journal of the American Chemical Society.
Original publication:
Asfandyar Sikandar, Laura Franz, Okke Melse, Iris Antes and Jesko Koehnke: Thiazoline-Specific Amidohydrolase PurAH Is the Gatekeeper of Bottromycin Biosynthesis. J. Am. Chem. Soc. 2019, DOI: 10.1021/jacs.8b12231
